RPE65-related dominant retinopathy

MONDO:0100452

A retinopathy caused by a heterozygous gain of function variant in the RPE65 gene.

Also known as: RP87, dominant RPE65 retinopathy, retinitis pigmentosa 87 with choroidal involvement

25 clinical trials for this condition and its sub-types, 0 tagged with RPE65-related dominant retinopathy itself.

Where it sits in the disease tree

Part of

Sub-types of RPE65-related dominant retinopathy

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